Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Starcraft is recalling certain 2022 Autumn Ridge Outfitter, Super Lite, and Super Lite Maxx travel trailers because the electric retractable awning's welded seam may separate, causing the awning to drop.
Charles Machine Works is recalling 2020-2022 Ditch Witch VT12, VT14, VT24, and VT14MV trailers because the vehicle certification labels list the wrong Gross Axle Weight Rating.
Highland Ridge RV is recalling 2,448 2022 model year trailers because a welded seam on the electric retractable awning fabric may separate, allowing the awning to drop unexpectedly.
Certain 2022 Land Rover Range Rover Velar vehicles were manufactured without an Audio Amplifier Module, causing loss of critical safety features including seat belt reminders and ADAS warnings. Owners should contact Land Rover at 1-800-637-6837 for free repair.
Pleasure Way recalls 2021-2022 Plateau motorhomes due to a mislabeled electrical circuit that can overload, causing wiring to overheat and creating a fire risk.
PACCAR is recalling approximately 630 2022-2023 Kenworth T680 tractor trailers. The mud flap may contact the fuel tank during operation, causing wear that could result in fuel spillage and increase crash or injury risk.
Newmar is recalling certain 2022 and 2021-2023 motorhomes due to improperly connected LPG service valves that may leak propane. A leak in the presence of an ignition source can increase fire risk.
Jayco is recalling specific 2022-2024 travel trailers and fifth wheels because a welded seam on the electric retractable awning may separate, causing the awning to drop.
Makita U.S.A. Inc. is recalling about 2,600 cordless hedge trimmers because the teal-colored guard on the shear blade may be missing, posing a laceration hazard to users.
Jubilant Cadista is recalling 9,600 bottles of Irbesartan Tablets (150mg) nationwide due to failed dissolution specifications. Affected lot IB220023A expires 08/2022.
Dole Fresh Vegetables is recalling Simply Nature Organic Spring Mix and Marketside Spring Mix due to potential contamination with hairy nightshade. The recalled products were distributed to Ohio, Illinois, Indiana, and Tennessee.
Medtronic is recalling three Cobalt Implantable Cardioverter Defibrillators (CRT-D) due to a manufacturing error that may have resulted in a cathode component being out of specification. Affected patients should contact their physician.
Abbott Laboratories is recalling the Alinity c Hemoglobin Reagent Kit because the ARCHITECT and Alinity c assays can generate falsely elevated Hemoglobin A1c results.
NuVasive Simplify Disc cervical implants have UDI barcodes with incorrect Global Trade Item Numbers that may cause selection of the wrong device size during implant surgery.
Eat Just, Inc. is recalling Just Egg Spring Greens due to potential Listeria monocytogenes contamination. The affected product was distributed in California, Georgia, and Texas.
Medline Industries is recalling 1,880 units of skin prep convenience kits with models DYNDP1127A and DYNDP1131 distributed nationwide due to leaking bottles of isopropyl alcohol.
Abbott Laboratories is recalling hemoglobin A1c test reagents used with ARCHITECT and Alinity c analyzers. The assay may produce falsely elevated A1c results, potentially affecting diabetes patient management.
Intuitive Surgical is recalling 62,895 Da Vinci S/Si Clip Appliers worldwide due to potential unexpected motion from partial instrument disengagement. No injuries or illnesses have been reported.
GE Healthcare's Centricity PACS software version 7.0 SP0.0.4.7 does not alert users when previously verified imaging studies are modified, potentially causing clinicians to use outdated or changed data without awareness.
Medline convenience kits containing leaking bottles of isopropyl alcohol are being recalled. Approximately 477 units were distributed nationwide and should not be used.
The Sight OLO automated hematology analyzer displays mixed-up default reference ranges for children ages 2-11 in software versions 2.63, 2.63.1, and 2.63.1.1, which could cause test results to appear incorrectly normal or abnormal.
Medline Industries is recalling medical device kits nationwide due to leaking isopropyl alcohol bottles. Approximately 28,745 units are affected. Consumers should stop using affected kits and contact the manufacturer.
Touch US Llc recalled 149 etouchus blood glucose meters (model ETM-G01) because they were marketed without FDA 510(k) clearance or approval. The device was distributed nationwide.
Dr. Reddy's Laboratories is recalling Lansoprazole 15-mg delayed-release tablets nationwide due to failed dissolution specifications. The tablets may not dissolve properly, potentially affecting medication effectiveness.
Medline has recalled custom neurosurgical procedure kits nationwide due to leaking bottles of isopropyl alcohol. The leakage poses a risk of contamination and chemical exposure during surgical procedures.